Bhattacharyya Dhananjay, Halder Sukanya, Basu Sankar, Mukherjee Debasish, Kumar Prasun, Bansal Manju
Computational Science Division, Saha Institute of Nuclear Physics, 1/AF Bidhannagar, Kolkata, 700064, India.
Computational Biophysics, IFM, Bioinformatics Division, University of Linkoping, 581 83, Linköping, Sweden.
J Comput Aided Mol Des. 2017 Feb;31(2):219-235. doi: 10.1007/s10822-016-0007-0. Epub 2017 Jan 19.
Comprehensive analyses of structural features of non-canonical base pairs within a nucleic acid double helix are limited by the availability of a small number of three dimensional structures. Therefore, a procedure for model building of double helices containing any given nucleotide sequence and base pairing information, either canonical or non-canonical, is seriously needed. Here we describe a program RNAHelix, which is an updated version of our widely used software, NUCGEN. The program can regenerate duplexes using the dinucleotide step and base pair orientation parameters for a given double helical DNA or RNA sequence with defined Watson-Crick or non-Watson-Crick base pairs. The original structure and the corresponding regenerated structure of double helices were found to be very close, as indicated by the small RMSD values between positions of the corresponding atoms. Structures of several usual and unusual double helices have been regenerated and compared with their original structures in terms of base pair RMSD, torsion angles and electrostatic potentials and very high agreements have been noted. RNAHelix can also be used to generate a structure with a sequence completely different from an experimentally determined one or to introduce single to multiple mutation, but with the same set of parameters and hence can also be an important tool in homology modeling and study of mutation induced structural changes.
对核酸双螺旋中非经典碱基对结构特征的全面分析受到少量三维结构的限制。因此,迫切需要一种用于构建包含任何给定核苷酸序列和碱基配对信息(无论是经典的还是非经典的)的双螺旋模型的程序。在此,我们描述了一个程序RNAHelix,它是我们广泛使用的软件NUCGEN的更新版本。该程序可以使用二核苷酸步长和碱基对取向参数,为具有定义的沃森-克里克或非沃森-克里克碱基对的给定双螺旋DNA或RNA序列重新生成双链体。如相应原子位置之间的小均方根偏差(RMSD)值所示,双螺旋的原始结构和相应的重新生成结构非常接近。已经重新生成了几种常见和不常见双螺旋的结构,并根据碱基对RMSD、扭转角和静电势将其与原始结构进行了比较,发现一致性非常高。RNAHelix还可用于生成与实验确定的序列完全不同的结构,或引入单突变至多突变,但使用相同的参数集,因此也可成为同源建模和突变诱导结构变化研究的重要工具。